HomeSwedenPERMOBIL, INC.

PERMOBIL, INC.

Sweden · Sundsvall Vasternorrland
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Brazil, South Korea, Australia, Israel — 5 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
n/aThis registry lists domestic registrants only
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
22listed device types
Class I 20Class II 2Class III 0
plus 45 registration records and 15 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
2registered devices
Class I 2
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
3GMP quality-system certificates
Import 3
AUAustraliaTGA ARTG
2active ARTG entries
Class I 2
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
1registrations
RURussiaRoszdravnadzor
pendingnot queried
Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States45 registration records, 15 510(k), 0 PMA, 3 excluded
Brazil2 confirmed, 0 excluded
Manufacturer names merged into this page: PERMOBIL AB · PERMOBIL, INC. · PERMOBIL, INC

Company information

Country
Sweden
City
Sundsvall Vasternorrland

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA 510(k) clearances by year

11990
11994
11997
11999
12000
22004
12007
12008
12011
12013
22015
12019
12020

FDA listed device types

showing 8 of 22
Attachment, Narrowing, Wheelchair 1Device, Anti-Tip, Wheelchair 1Armrest, Wheelchair 1Footrest, Wheelchair 1Restraint, Wheelchair, Non-Protective 1Components, Wheelchair 1Belt, Wheelchair 1Climber, Curb, Wheelchair 1

Registration details (sample)

MarketIdentifierNameClass / date
USK190682Explorer Mini2020-02-27
USK191874F5 Corpus VS2019-10-25
USK143180F32015-03-27
BR80626470007Cadeiras de RodasClass I
BR80626470008Cadeira de RodasClass I

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